Gene-specific Copy Number Variation Probe-CYP26B1
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| Catalog: |
CNVFP-CYP26B1-03379 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CYP26B1). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
CYP26B1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CYP26B1 genes. This product achieves the purpose of detection by hybridizing with the CYP26B1 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Cytochrome P450 Family 26 Subfamily B Member 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the cytochrome P450 superfamily. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The encoded protein is localized to the endoplasmic reticulum, and functions as a critical regulator of all-trans retinoic acid levels by the specific inactivation of all-trans retinoic acid to hydroxylated forms. Mutations in this gene are associated with radiohumeral fusions and other skeletal and craniofacial anomalies, and increased levels of the encoded protein are associated with atherosclerotic lesions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013] |
| Gene Symbol |
CYP26B1 |
| Location |
2p13.2 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 72356366-72374963 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-CYP26B1-03379-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CYP26B1-03379-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CYP26B1-03379-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CYP26B1-03379-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CYP26B1-03379-AQ |
467nm |
418nm |
|
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